Execution of product development stage experimental activities (API characterization, Pre-formulation studies, formulation and process development, stability studies, scaleup, and dossier batches activities )
Follow and ensure compliance with Good documentation, cGMP & regulatory requirements for Formulation activities.
Executing formulation activities as per production requirements and timelines.
Qualification & Calibration activities.
Preparation of System and Equipment related SOP.
Working on Technical documentation & Protocols for executions.
Establishing In-house systems and procedures to ensure cGMP practices & regulatory requirements.
Submission and handling of analytical samples.
Any other specific functional activities defined on a case-to-case basis
Preparation, documentation, and follow-ups for the approval of lab scale-related activities.
To report to the superior in a timely manner.
To complete all tasks and assignments given by the superior.
To attend ad-hoc request.
Work rights
The opportunity is available to applicants in any of the following categories.